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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838523Generated: October 31, 2026

Potassium Carbonate → 4-(3-Acetoxy-4-methylanilino)-6-methoxy-7-(2-methoxyethoxy)quinazoline

https://huagongshe.com/reaction/1838523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromoethyl methyl etherHCID 80972—
Reactant4-(3-Acetoxy-4-methylanilino)-7-hydroxy-6-methoxyquinazolineHCID 135450804—
SolventDimethylformamideHCID 6228—
Product4-(3-Acetoxy-4-methylanilino)-6-methoxy-7-(2-methoxyethoxy)quinazolineHCID 2247823384.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

Potassium carbonate (2.2 g, 16 mmol) was added to a solution of 4-(3-acetoxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline (1.51 g, 4 mmol) in DMF (30 ml) and the mixture stirred for 15 minutes. 2-Bromoethyl methyl ether (667 mg, 4.8 mmol) was then added dropwise. The mixture was stirred for 1 hour at ambient temperature, then heated at 60° C. for 17 hours and finally allowed to cool. The insoluble material was removed by filtration and the filter pad washed with DMF. The filtrate was partitioned between ethyl acetate and water, the organic layer was separated, washed with brine, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with methylene chloride/methanol (95/5 followed by 93/7). The purified product was triturated with ether to give 4-(3-acetoxy-4-methylanilino)-6-methoxy-7-(2-methoxyethoxy)quinazoline (1.34 g, 84%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673803B2
Source datasetuspto-grants-2004_01
ORD IDord-8f9d1fdf2f8d41bb8aad3698f5ce8ca4
Source noteuspto-grants-2004_01